venlafaxine hydrochloride

Generic: venlafaxine hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name venlafaxine hydrochloride
Generic Name venlafaxine hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

venlafaxine hydrochloride 75 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8140
Product ID 68788-8140_007d0508-5680-41b6-ba36-4c9cc4dd828f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200834
Listing Expiration 2026-12-31
Marketing Start 2022-02-11

Pharmacologic Class

Classes
norepinephrine uptake inhibitors [moa] serotonin uptake inhibitors [moa] serotonin and norepinephrine reuptake inhibitor [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888140
Hyphenated Format 68788-8140

Supplemental Identifiers

RxCUI
313585
UNII
7D7RX5A8MO

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name venlafaxine hydrochloride (source: ndc)
Generic Name venlafaxine hydrochloride (source: ndc)
Application Number ANDA200834 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-3)
  • 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-6)
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-9)
source: ndc

Packages (3)

68788-8140-3 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-3) 68788-8140-6 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-6) 68788-8140-9 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-9)

Ingredients (1)

venlafaxine hydrochloride (75 mg/1)

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "007d0508-5680-41b6-ba36-4c9cc4dd828f", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["22980b32-cbae-4f37-9fc0-b47221b2c32e"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-3)", "package_ndc": "68788-8140-3", "marketing_start_date": "20220211"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-6)", "package_ndc": "68788-8140-6", "marketing_start_date": "20220211"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8140-9)", "package_ndc": "68788-8140-9", "marketing_start_date": "20220211"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8140_007d0508-5680-41b6-ba36-4c9cc4dd828f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8140", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20220211", "listing_expiration_date": "20261231"}